Manufacturing Validation Engineer - cGMP & Equipment

Scorpion Therapeutics; Wisconsin; On-site; USD 65,000 - 95,000; Full time

Job summary

Scorpion Therapeutics in Wisconsin seeks a Validation professional to support qualification, validation, and compliance in a regulated manufacturing environment. You will evaluate protocols, troubleshoot validation issues, and write technical reports.

The role requires a degree with experience or equivalent, strong FDA/GxP knowledge, data analysis skills (Excel), and excellent communication. On‑premise work with potential off-hours and adherence to cGMP.

Qualifications

• Bachelor's degree or equivalent experience in a regulated field.
• Experience with FDA regulations, GxP, and validation principles.
• Proficiency in data analysis and Excel for validation work.

Responsibilities

• Evaluate and review protocols, troubleshoot validation issues, and write technical reports.
• Contribute to validation projects and ensure cGMP compliance.
• Collaborate with cross-functional teams in a regulated manufacturing environment.

Skills

Data analysis

Excel proficiency

Education

Bachelor's degree in a relevant field

Associate's degree with 4+ years

High school diploma with 6+ years

Job description

Scorpion Therapeutics in Wisconsin seeks a Validation professional to support qualification, validation, and compliance in a regulated manufacturing environment. You will evaluate protocols, troubleshoot validation issues, and write technical reports.

The role requires a degree with experience or equivalent, strong FDA/GxP knowledge, data analysis skills (Excel), and excellent communication. On‑premise work with potential off-hours and adherence to cGMP.